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Chemical Structure| 96-76-4 Chemical Structure| 96-76-4
Chemical Structure| 96-76-4

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2,4-Di-tert-butylphenol is an endogenous metabolite.

Synonyms: 2,4-DTBP

4.5 *For Research Use Only !

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Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

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Product Details of 2,4-Di-tert-butylphenol

CAS No. :96-76-4
Formula : C14H22O
M.W : 206.32
SMILES Code : OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C
Synonyms :
2,4-DTBP
MDL No. :MFCD00008828
InChI Key :ICKWICRCANNIBI-UHFFFAOYSA-N
Pubchem ID :7311

Safety of 2,4-Di-tert-butylphenol

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H410
Precautionary Statements:P273-P280-P305+P351+P338
Class:8
UN#:2430
Packing Group:

Application In Synthesis of 2,4-Di-tert-butylphenol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 96-76-4 ]
  • Downstream synthetic route of [ 96-76-4 ]

[ 96-76-4 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 96-76-4 ]
  • [ 31570-04-4 ]
YieldReaction ConditionsOperation in experiment
98.3%
Stage #1: With pyridine In methanol; toluene at 5 - 40℃;
Stage #2: With phosphorus trichloride In methanol; toluene at 95℃; for 0.5 h;
(1)First, 11.0 g of 2,4-di-tert-butylphenol was added to a three-necked flask.a diatomaceous earth-supported pyridine catalyst of 22 mg and a mixed solution of methanol and toluene in 400 mL, and then added to the rotor, and a reflux condenser,The thermometer and the dropping funnel were fixed on a three-necked flask;(2)The three-necked flask containing the reactant in the step (1) was heated under an oil bath condition at a rate of 5 degrees Celsius per ten minutes.Raise the temperature to 40 ° C,Reacting solution;(3)To the reaction liquid of the step (2), 5.57 g of phosphorus trichloride dissolved in 30 mL of toluene was added dropwise to control the dropping rate.After 15 minutes of dropwise addition, continue to heat up to 95 ° C,The reaction was kept for 30 minutes, and the solvent was distilled off under reduced pressure.Recrystallization from n-hexane,That is, the product is obtained.The yield of the final product was 98.3percent.The purity was 98.9percent.
References: [1] Patent: CN108467406, 2018, A, . Location in patent: Paragraph 0038-0040; 0044-0046; 0050-0052; 0056-0058; 0062.
[2] Patent: CN109593101, 2019, A, . Location in patent: Paragraph 0024-0030.
  • 2
  • [ 98-54-4 ]
  • [ 96-76-4 ]
  • [ 31570-04-4 ]
  • [ 4235-89-6 ]
  • [ 1000027-03-1 ]
  • [ 161519-57-9 ]
References: [1] Patent: WO2011/14527, 2011, A2, . Location in patent: Page/Page column 36; 37.
  • 3
  • [ 95-47-6 ]
  • [ 96-76-4 ]
  • [ 298-12-4 ]
  • [ 164391-52-0 ]
References: [1] Patent: US6359148, 2002, B1, . Location in patent: Page column 40 - 41.
  • 4
  • [ 96-76-4 ]
  • [ 164391-52-0 ]
References: [1] Synthesis, 2004, # 2, p. 249 - 254.
[2] Synlett, 1999, # SPEC. ISS., p. 863 - 864.
 

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